| Literature DB >> 35000107 |
Nida N Farshori1, Maqsood A Siddiqui2, Mai M Al-Oqail1, Ebtesam S Al-Sheddi1, Shaza M Al-Massarani1, Maqusood Ahamed3, Javed Ahmad4, Abdulaziz A Al-Khedhairy4.
Abstract
Copper oxide nanoparticles (CuONPs) are purposefully used to inhibit the growth of bacteria, algae, and fungi. Several studies on the beneficial and harmful effects of CuONPs have been conducted in vivo and in vitro, but there are a few studies that explain the toxicity of CuONPs in human airway epithelial cells (HEp-2). As a result, the purpose of this study is to look into the dose-dependent toxicity of CuONPs in HEp-2 cells. After 24 h of exposure to 1-40 µg/ml CuONPs, the MTT and neutral red assays were used to test for cytotoxicity. To determine the mechanism(s) of cytotoxicity in HEp-2 cells, additional oxidative stress assays (LPO and GSH), the amount of ROS produced, the loss of MMP, caspase enzyme activities, and apoptosis-related genes were performed using qRT-PCR. CuONPs exhibited dose-dependent cytotoxicity in HEp-2 cells, with an IC50 value of ~ 10 μg/ml. The morphology of HEp-2 cells was also altered in a dose-dependent manner. The involvement of oxidative stress in CuONP-induced cytotoxicity was demonstrated by increased LPO levels and ROS generation, as well as decreased levels of GSH and MMP. Furthermore, activated caspase enzymes and altered apoptotic genes support CuONPs' ability to induce apoptosis in HEp-2 cells. Overall, this study demonstrated that CuONPs can cause apoptosis in HEp-2 cells via oxidative stress; therefore, CuONPs may pose a risk to human health and should be handled and used with caution.Entities:
Keywords: Caspase activity; Copper oxide nanoparticles; Cytotoxicity; Gene expression; HEp-2 cells; Oxidative stress
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Year: 2022 PMID: 35000107 DOI: 10.1007/s12011-022-03107-8
Source DB: PubMed Journal: Biol Trace Elem Res ISSN: 0163-4984 Impact factor: 4.081